Use Your Power for Purpose

Every day, our unwavering commitment to quality ensures the delivery of safe and effective products to patients. Our flexible, innovative, and customer-oriented culture is rooted in science and risk-based compliance. By being part of our team, you help uphold a quality culture that adapts and evolves to meet the needs of patients, ensuring that every product we deliver is of the highest standard. Your role is crucial in maintaining this commitment and driving forward our mission to improve patient outcomes.

What You Will Achieve

In this role, you will:

Ensure the application of established quality systems to meet Pfizer and regulatory authority requirements for on-site finished product manufacturing. Ensure that GMP standards, as applicable to each specific product, are consistently met and that the site remains in full compliance with Pfizer and regulatory expectations. Manage, investigate, review and follow on site quality deviation report's approvalReview laboratory investigation reports  Address customer complaints Follow on external deviation such as temperature excursions of imported materials or exported productsMonitor and review CAPAs and commitments resulting from investigations Create, update, and approve QA-controlled documentsPrepare, follow up and communicate monthly quality performance metricsOrganize, prepare and partipate in monthly SQRT (Site Quality Review Team) meetingsParticipate in internal and external auditsContribute in NTM - Notification to Management process Prepare and review AQRT (Area Quality Review Team) reports following NTMHere Is What You Need (Minimum Requirements)​​Bachelor's + 5 or Degree in Pharmacy, Biology, Chemistry, or equivalent fieldExperience in pharmaceutical industry / quality assurance or a similar regulated environmentStrong knowledge of GMP, regulatory compliance, and quality systemsExcellent analytical, organizational, and communication skillsFluent English and French

Bonus Points If You Have (Preferred Requirements)

Experience at a manufacturing siteManaging and writing deviationsExperience in production batch record review, Enterprise Resource Planning system, investigation of non-conformance, root cause analysis and change control managementStrong problem-solving skillsAbility to work independently and as part of a teamExcellent time management and multitasking abilities  
Work Location Assignment: On Premise

Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.

Quality Assurance and Control

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